Canonical Allele Identifier: CA15794438
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs2770304

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46881230C>T , CM000675.2:g.46881230C>T GRCh38
NC_000013.10:g.47455365C>T , CM000675.1:g.47455365C>T GRCh37
NC_000013.9:g.46353366C>T NCBI36
NG_013011.1:g.20805G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000542664.4:c.613+11160G>A MANE Select ENSP00000437737.1:p.=
ENST00000543956.5:c.124+11160G>A ENSP00000441861.2:p.=
ENST00000378688.8:c.613+11160G>A ENSP00000367959.3:p.=
ENST00000542664.3:c.613+11160G>A ENSP00000437737.1:p.=
ENST00000543956.4:c.361+11160G>A ENSP00000441861.1:p.=
NM_000621.4:c.613+11160G>A NP_000612.1:p.=
NM_001165947.2:c.361+11160G>A NP_001159419.1:p.=
NM_000621.5:c.613+11160G>A MANE Select NP_000612.1:p.=
NM_001165947.5:c.124+11160G>A NP_001159419.2:p.=
NM_001378924.1:c.613+11160G>A NP_001365853.1:p.=